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Regulation of the expression of the liver cancer susceptibility gene MICA by microRNAs.


ABSTRACT: Hepatocellular carcinoma (HCC) is a threat to public health worldwide. We previously identified the association of a single nucleotide polymorphism (SNP) at the promoter region of the MHC class I polypeptide-related sequence A (MICA) gene with the risk of hepatitis-virus-related HCC. Because this SNP affects MICA expression levels, regulating MICA expression levels may be important in the prevention of HCC. We herein show that the microRNA (miR) 25-93-106b cluster can modulate MICA levels in HCC cells. Overexpression of the miR 25-93-106b cluster significantly suppressed MICA expression. Conversely, silencing of this miR cluster enhanced MICA expression in cells that express substantial amounts of MICA. The changes in MICA expression levels by the miR25-93-106b cluster were biologically significant in an NKG2D-binding assay and an in vivo cell-killing model. These data suggest that the modulation of MICA expression levels by miRNAs may be a useful method to regulate HCCs during hepatitis viral infection.

SUBMITTER: Kishikawa T 

PROVIDER: S-EPMC3781398 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Regulation of the expression of the liver cancer susceptibility gene MICA by microRNAs.

Kishikawa Takahiro T   Otsuka Motoyuki M   Yoshikawa Takeshi T   Ohno Motoko M   Takata Akemi A   Shibata Chikako C   Kondo Yuji Y   Akanuma Masao M   Yoshida Haruhiko H   Koike Kazuhiko K  

Scientific reports 20130101


Hepatocellular carcinoma (HCC) is a threat to public health worldwide. We previously identified the association of a single nucleotide polymorphism (SNP) at the promoter region of the MHC class I polypeptide-related sequence A (MICA) gene with the risk of hepatitis-virus-related HCC. Because this SNP affects MICA expression levels, regulating MICA expression levels may be important in the prevention of HCC. We herein show that the microRNA (miR) 25-93-106b cluster can modulate MICA levels in HCC  ...[more]

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